A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658426



Internal ID9577845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85366184..85378701hg38UCSC Ensembl
Outerchr8:85366147..85378751hg38UCSC Ensembl
Innerchr8:86278413..86290930hg19UCSC Ensembl
Outerchr8:86278376..86290980hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3812605
hg1912605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6155200
SamplesNA18608
Known GenesCA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658426
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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